Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11958933
rs11958933
1 1.000 0.040 5 25323598 intron variant G/A snv 0.70 0.700 1.000 1 2017 2017
dbSNP: rs931924
rs931924
1 1.000 0.040 5 25321925 intron variant C/T snv 0.70 0.700 1.000 1 2017 2017